Canonical Allele Identifier: CA492076004
Gene: RLBP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.89755012G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89211781G>T , CM000677.2:g.89211781G>T GRCh38
NC_000015.9:g.89755012G>T , CM000677.1:g.89755012G>T GRCh37
NC_000015.8:g.87556016G>T NCBI36
NG_008116.1:g.14911C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000268125.10:c.646C>A MANE Select ENSP00000268125.5:p.Arg216=
ENST00000268125.9:c.646C>A ENSP00000268125.5:p.Arg216=
ENST00000563254.1:c.63C>A
ENST00000567787.1:c.*224C>A ENSP00000457251.1:n.*224C>A
NM_000326.4:c.646C>A NP_000317.1:p.Arg216=
XM_011521870.1:c.646C>A XP_011520172.1:p.Arg216=
XM_011521871.1:c.571C>A XP_011520173.1:p.Arg191=
XM_011521872.1:c.571C>A XP_011520174.1:p.Arg191=
XM_011521870.2:c.646C>A XP_011520172.1:p.Arg216=
XM_017022460.1:c.673C>A XP_016877949.1:p.Arg225=
NM_000326.5:c.646C>A MANE Select NP_000317.1:p.Arg216=